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- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion type Assertion NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_head.
- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion wasGeneratedBy ECO_0000203 NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_provenance.
- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion wasDerivedFrom befree-20150227 NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_provenance.
- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion SIO_000772 19073947 NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_provenance.
- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion evidence source_evidence_literature NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_provenance.
- NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_assertion description "[Mutations in FLNA (Xq28) and ARFGEF2 (20q13) are responsible for X-linked bilateral PH and a rare autosomal recessive form of PH with microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847372.RAcYMj-HsETicdiBZyR4O7JuParD-VrXSUKN0UW8AGBu4130_provenance.