Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_assertion description "[In addition, six previously reported (p.R48G, p.A119S, p.V432L, p.D449D, p.N453S, and 372-12C>T in intron 1) and four novel (p.V395V, p.P400P, p.V518A, and c.2016C>G in the 3'-UTR) single nucleotide polymorphism (SNPs) were also observed in POAG patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_assertion evidence source_evidence_literature NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_assertion SIO_000772 16688110 NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_assertion wasDerivedFrom befree-20140225 NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_assertion wasGeneratedBy ECO_0000203 NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629511.RAPfdRxD19tBUdL_fWR7PltN649UqoZPxGbfd_GO-2ZAY130_provenance.