Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_assertion description "[A total of 1,250 patients with NSCLC were screened for EGFR mutations at a single institution between March 2006 and May 2010.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_assertion evidence source_evidence_literature NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_assertion SIO_000772 25422153 NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_assertion wasDerivedFrom befree-2016 NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_assertion wasGeneratedBy ECO_0000203 NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1239749.RABBe7w0pG6zbxQeLZQyk4oadyHWkJrC72uxETsy695u4130_provenance.