Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_assertion description "[Our study demonstrates that mutations in each part of the EGFR pathway were associated with different clinicopathologic features in patients with NSCLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_assertion evidence source_evidence_literature NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_assertion SIO_000772 20881644 NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_assertion wasDerivedFrom gad-20130706 NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_assertion wasGeneratedBy ECO_0000203 NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64410.RArDkBshCnSv9vK2BppCv48kjVriUOVeUDCAgox86BN_g130_provenance.