Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_assertion wasGeneratedBy ECO_0000203 NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_assertion wasDerivedFrom befree-20150227 NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_assertion SIO_000772 25098561 NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_assertion evidence source_evidence_literature NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_assertion description "[Using a linkage analysis and a candidate gene approach, two genes have been implicated in congenital MRMV disorder to date: DCC on 18q21.2 (MRMV1), which encodes a netrin receptor, and RAD51 on 15q15.1 (MRMV2), which is involved in the maintenance of genomic integrity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.