o
cc
Subject
[BIONT] BIONT ACPP Collaboration on extending Parkinson's Disease Use Case
to the Bedside
Phone
+1 617 761 6200, conference 24668 ("BIONT")
IRC
irc://irc.w3.org:6665/hcls
Browser-based IRC client
http://www.w3.org/2001/01/cgi-irc
Date and Time: 12th De
he current Parkinson's
Disease Use Case to the Bedside.
---Vipul
===
Vipul Kashyap, Ph.D.
Senior Medical Informatician
Clinical Informatics R&D, Partners HealthCare System
Phone: (781)416-9254
Cell: (617)943-7120
http://www.partners.org/ci
arkinson's
Disease Use Case to the Bedside.
---Vipul
===
Vipul Kashyap, Ph.D.
Senior Medical Informatician
Clinical Informatics R&D, Partners HealthCare System
Phone: (781)416-9254
Cell: (617)943-7120
http://www.partners.org/cird/AboutUs.
On Mar 10, 2006, at 2:57 PM, Brian Osborne wrote:
Eric M.,
I'm looking at the Piggy Bank scrapers at
http://potlach.org/2005/10/scrapers/, I think we want to create an
additional one that uses the results of an NCBI eutils query, the
PubMed one
is not well suited for the "Gene Neural relate
Brian,
I think using the eutils query is a good first step for retrieving XML to
be converted to RDF, so I applaud your offer, and look forwards to us
using it.
cheers,
Eric
--- Brian Osborne <[EMAIL PROTECTED]> wrote:
>
> Eric M.,
>
> I'm looking at the Piggy Bank scrapers at
> http://potla
Eric M.,
I'm looking at the Piggy Bank scrapers at
http://potlach.org/2005/10/scrapers/, I think we want to create an
additional one that uses the results of an NCBI eutils query, the PubMed one
is not well suited for the "Gene Neural related gene data" and "Protein
Neural related protein data" t
On Mar 6, 2006, at 2:36 PM, Eric Neumann wrote:
I have added a Parkinson's Disease (PD) information aggregation use-
case on the wiki site:
http://esw.w3.org/topic/ParkinsonsDisease
Currently it has disease related information on implicated genes,
causes, treatments, inheritance, and pa
I have added a Parkinson's Disease (PD) information aggregation use-case on the
wiki site:
http://esw.w3.org/topic/ParkinsonsDisease
Currently it has disease related information on implicated genes, causes,
treatments, inheritance, and pathways. It eventually is to serve as a resource
for one
