Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_assertion description "[Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_assertion evidence source_evidence_literature NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_assertion SIO_000772 10554356 NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_assertion wasDerivedFrom befree-2016 NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_assertion wasGeneratedBy ECO_0000203 NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.
- befree-2016 importedOn "2016-02-19" NP267253.RAG4F4WNqrRlg-iPiL9VsIbBlBwsXVZO9dj84yZhSBNfw130_provenance.