Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_assertion description "[SMARCD1 was mapped to the critical region of Allgrove syndrome; however, no mutation was identified in one Allgrove syndrome family studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_assertion evidence source_evidence_literature NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_assertion SIO_000772 9693044 NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_assertion wasDerivedFrom befree-20140225 NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_assertion wasGeneratedBy ECO_0000203 NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384031.RAyKn4auP5oe4H2gBnGS_Ox8YtghhU3v0zk7ml8aDpzmw130_provenance.