Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_assertion wasGeneratedBy ECO_0000203 NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_assertion wasDerivedFrom befree-20150227 NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_assertion SIO_000772 22344793 NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_assertion evidence source_evidence_literature NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.
- NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_assertion description "[Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530089.RA1K9d5fiF8ci-Ger3MBglRlwtgr3cqwrS1ioQ4lnJWRE130_provenance.