Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_assertion description "[LIPH is a second causative gene for ARWH/hypotrichosis, giving rise to a phenotype clinically indistinguishable from P2RY5 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_assertion evidence source_evidence_literature NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_assertion SIO_000772 18830268 NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_assertion wasDerivedFrom lhgdn-20090331 NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_assertion wasGeneratedBy ECO_0000203 NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP242540.RAGJpoXvqhwyt-Z4_X6Ic9A3mXBM1Hz5yVs6c0h-Wr4jw130_provenance.